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The endosomal transcriptional regulator RNF11 integrates degradation and transport of EGFR
Stimulation of cells with epidermal growth factor (EGF) induces internalization and partial degradation of the EGF receptor (EGFR) by the endo-lysosomal pathway. For continuous cell functioning, EGFR plasma membrane levels are maintained by transporting newly synthesized EGFRs to the cell surface. T...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119934/ https://www.ncbi.nlm.nih.gov/pubmed/27872256 http://dx.doi.org/10.1083/jcb.201601090 |
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author | Scharaw, Sandra Iskar, Murat Ori, Alessandro Boncompain, Gaelle Laketa, Vibor Poser, Ina Lundberg, Emma Perez, Franck Beck, Martin Bork, Peer Pepperkok, Rainer |
author_facet | Scharaw, Sandra Iskar, Murat Ori, Alessandro Boncompain, Gaelle Laketa, Vibor Poser, Ina Lundberg, Emma Perez, Franck Beck, Martin Bork, Peer Pepperkok, Rainer |
author_sort | Scharaw, Sandra |
collection | PubMed |
description | Stimulation of cells with epidermal growth factor (EGF) induces internalization and partial degradation of the EGF receptor (EGFR) by the endo-lysosomal pathway. For continuous cell functioning, EGFR plasma membrane levels are maintained by transporting newly synthesized EGFRs to the cell surface. The regulation of this process is largely unknown. In this study, we find that EGF stimulation specifically increases the transport efficiency of newly synthesized EGFRs from the endoplasmic reticulum to the plasma membrane. This coincides with an up-regulation of the inner coat protein complex II (COPII) components SEC23B, SEC24B, and SEC24D, which we show to be specifically required for EGFR transport. Up-regulation of these COPII components requires the transcriptional regulator RNF11, which localizes to early endosomes and appears additionally in the cell nucleus upon continuous EGF stimulation. Collectively, our work identifies a new regulatory mechanism that integrates the degradation and transport of EGFR in order to maintain its physiological levels at the plasma membrane. |
format | Online Article Text |
id | pubmed-5119934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51199342017-05-21 The endosomal transcriptional regulator RNF11 integrates degradation and transport of EGFR Scharaw, Sandra Iskar, Murat Ori, Alessandro Boncompain, Gaelle Laketa, Vibor Poser, Ina Lundberg, Emma Perez, Franck Beck, Martin Bork, Peer Pepperkok, Rainer J Cell Biol Research Articles Stimulation of cells with epidermal growth factor (EGF) induces internalization and partial degradation of the EGF receptor (EGFR) by the endo-lysosomal pathway. For continuous cell functioning, EGFR plasma membrane levels are maintained by transporting newly synthesized EGFRs to the cell surface. The regulation of this process is largely unknown. In this study, we find that EGF stimulation specifically increases the transport efficiency of newly synthesized EGFRs from the endoplasmic reticulum to the plasma membrane. This coincides with an up-regulation of the inner coat protein complex II (COPII) components SEC23B, SEC24B, and SEC24D, which we show to be specifically required for EGFR transport. Up-regulation of these COPII components requires the transcriptional regulator RNF11, which localizes to early endosomes and appears additionally in the cell nucleus upon continuous EGF stimulation. Collectively, our work identifies a new regulatory mechanism that integrates the degradation and transport of EGFR in order to maintain its physiological levels at the plasma membrane. The Rockefeller University Press 2016-11-21 /pmc/articles/PMC5119934/ /pubmed/27872256 http://dx.doi.org/10.1083/jcb.201601090 Text en © 2016 Scharaw et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Scharaw, Sandra Iskar, Murat Ori, Alessandro Boncompain, Gaelle Laketa, Vibor Poser, Ina Lundberg, Emma Perez, Franck Beck, Martin Bork, Peer Pepperkok, Rainer The endosomal transcriptional regulator RNF11 integrates degradation and transport of EGFR |
title | The endosomal transcriptional regulator RNF11 integrates degradation and transport of EGFR |
title_full | The endosomal transcriptional regulator RNF11 integrates degradation and transport of EGFR |
title_fullStr | The endosomal transcriptional regulator RNF11 integrates degradation and transport of EGFR |
title_full_unstemmed | The endosomal transcriptional regulator RNF11 integrates degradation and transport of EGFR |
title_short | The endosomal transcriptional regulator RNF11 integrates degradation and transport of EGFR |
title_sort | endosomal transcriptional regulator rnf11 integrates degradation and transport of egfr |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119934/ https://www.ncbi.nlm.nih.gov/pubmed/27872256 http://dx.doi.org/10.1083/jcb.201601090 |
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